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Epilepsy of infancy with migrating focal seizures in a patient with nonketotic hyperglycinemia

Nonketotic hyperglycinemia (NKH) is an inborn error of glycine metabolism leading to refractory epilepsy and severe developmental delays. It is caused by autosomal recessive inheritance of a defect in the glycine cleavage system in the mitochondrial enzymatic complex pathway [1]. This defect le...

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Bibliographic Details
Main Authors: Anuar, Muhamad Azamin, Syed Ahmad Shihabuddin Abdurrahman Alsagoff, Sharifah Aishah, Mohamed, Ahmad Rithauddin, Murugesu, Sumitha
Format: Article
Language:English
Published: Korean Child Neurology Society 2022
Subjects:
RJ Pediatrics
RJ370 Disease of children
RJ58 Clinical cases
Online Access:http://irep.iium.edu.my/104286/2/104286_Epilepsy%20of%20Infancy%20with%20Migrating%20Focal%20Seizures.pdf
http://irep.iium.edu.my/104286/
https://www.annchildneurol.org/journal/view.php?doi=10.26815/acn.2022.00346
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http://irep.iium.edu.my/104286/2/104286_Epilepsy%20of%20Infancy%20with%20Migrating%20Focal%20Seizures.pdf
http://irep.iium.edu.my/104286/
https://www.annchildneurol.org/journal/view.php?doi=10.26815/acn.2022.00346

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